- This topic has 17 replies, 7 voices, and was last updated 10 years, 6 months ago by .
- You must be logged in to reply to this topic.
Wow! Thanks so much Dr Diana xxx I’m flattered by all this x
We are not just whistling Dixie here, my friend. We’re a supportive bunch, but we won’t LIE! 😉 You are incredibly talented. Have you considered selling prints of your work? 😉
Before I got really sick I used to run my own little business selling prints and phone skins from Instagram, not sure if you have heard of it before but I was doing very well with 8000 followers. Unfortunately though my pots took a turn for the worst and I haven’t drawn every day for a while I’m luck now to draw once or twice a month, my hands are not what they used to be.
To be honest it really hurts that I can’t do what I used too, don’t get me wrong i still love to draw but they take me much longer. I love the sport I get from my followers and they all know I’m ill and what’s wrong so it’s allowed me to spread more awareness of both pots and eds. I have some speed videos of me drawing and also vidoe blogs of how being chronically ill effects me.
Thanks so much for taking the time to write to me and read my long note xxx
Oh by the way if you wanted to see any more it’s carriejanesart in Facebook twitter and Instagram xxxx
This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.
“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”
-- Chris Gross